| Literature DB >> 31235846 |
Hui-Hui Liu1, Ye-Xuan Cao1, Di Sun1, Jing-Lu Jin1, Hui-Wen Zhang1, Yuan-Lin Guo1, Cheng-Gang Zhu1, Na-Qiong Wu1, Ying Gao1, Qiu-Ting Dong1, Jian-Jun Li2.
Abstract
High-sensitivity C-reactive protein (hsCRP), a marker of inflammation, can promote atherosclerosis and predict cardiovascular events. However, no data are currently available about the combined effects of hsCRP and hypertension on cardiovascular risk. This study sought to elucidate this matter. A total of 7325 consecutive patients with angina-like chest pain undergoing coronary angiography were evaluated, and 4291 patients with stable, newly diagnosed coronary artery disease (CAD) were enrolled. They were subdivided into three groups according to baseline hsCRP levels (<1, 1-3, and >3 mg/L) and further stratified by hypertension status. The severity of CAD was assessed by the Gensini score and number of diseased vessels. All participants were followed for the occurrence of cardiovascular events. The coronary severity and cardiovascular outcomes were compared among these groups. We observed 530 (12.35%) incident cardiovascular events over 14,210 person-years. Elevated hsCRP was associated with more severe coronary lesions (p < 0.05) and an elevated but nonsignificant increased risk of cardiovascular events (p > 0.05). When hypertension was included as a stratifying factor, both patients with high hsCRP and normal blood pressure and hypertensive patients with any level of hsCRP had more severe coronary lesions compared with the reference group with low hsCRP and normotension. However, compared with the reference group, the cardiovascular event risk was only significantly elevated in patients with high hsCRP and hypertension (p < 0.05). The combination of elevated hsCRP and hypertension greatly increased the cardiovascular risk in patients with stable, newly diagnosed CAD, supporting that hsCRP could be treated as a marker for stratification in high-risk patients.Entities:
Keywords: Coronary artery disease; Events; Hypertension; Inflammation; Risk factors
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Year: 2019 PMID: 31235846 DOI: 10.1038/s41440-019-0293-8
Source DB: PubMed Journal: Hypertens Res ISSN: 0916-9636 Impact factor: 3.872